美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
71610-424-30	71610-424	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20200507	N/A	ANDA	ANDA071322	Aphena Pharma Solutions - Tennessee, LLC	DIAZEPAM	10 mg/1	30 TABLET in 1 BOTTLE (71610-424-30)
71610-424-45	71610-424	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20220804	N/A	ANDA	ANDA071322	Aphena Pharma Solutions - Tennessee, LLC	DIAZEPAM	10 mg/1	45 TABLET in 1 BOTTLE (71610-424-45)
71610-424-53	71610-424	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20200507	N/A	ANDA	ANDA071322	Aphena Pharma Solutions - Tennessee, LLC	DIAZEPAM	10 mg/1	60 TABLET in 1 BOTTLE (71610-424-53)
71610-424-60	71610-424	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20200507	N/A	ANDA	ANDA071322	Aphena Pharma Solutions - Tennessee, LLC	DIAZEPAM	10 mg/1	90 TABLET in 1 BOTTLE (71610-424-60)
80425-0120-2	80425-0120	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	19861210	N/A	ANDA	ANDA071322	Advanced Rx Pharmacy of Tennessee, LLC	DIAZEPAM	10 mg/1	60 TABLET in 1 BOTTLE (80425-0120-2)
68071-4829-3	68071-4829	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20190402	N/A	ANDA	ANDA071322	NuCare Pharmaceuticals,Inc.	DIAZEPAM	10 mg/1	30 TABLET in 1 BOTTLE (68071-4829-3)
70518-0162-0	70518-0162	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20170123	N/A	ANDA	ANDA071322	REMEDYREPACK INC.	DIAZEPAM	10 mg/1	30 TABLET in 1 BLISTER PACK (70518-0162-0)
70518-0162-3	70518-0162	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20210528	N/A	ANDA	ANDA071322	REMEDYREPACK INC.	DIAZEPAM	10 mg/1	2 TABLET in 1 BOTTLE, PLASTIC (70518-0162-3)
70518-0162-4	70518-0162	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20240201	N/A	ANDA	ANDA071322	REMEDYREPACK INC.	DIAZEPAM	10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-0162-4)
71610-424-70	71610-424	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20200507	N/A	ANDA	ANDA071322	Aphena Pharma Solutions - Tennessee, LLC	DIAZEPAM	10 mg/1	120 TABLET in 1 BOTTLE (71610-424-70)
76420-784-90	76420-784	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20240308	N/A	ANDA	ANDA071322	Asclemed USA, Inc.	DIAZEPAM	10 mg/1	90 TABLET in 1 BOTTLE (76420-784-90)
0172-3927-60	0172-3927	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	19861210	N/A	ANDA	ANDA071322	Teva Pharmaceuticals USA, Inc.	DIAZEPAM	10 mg/1	100 TABLET in 1 BOTTLE (0172-3927-60)
0172-3927-70	0172-3927	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	19861210	N/A	ANDA	ANDA071322	Teva Pharmaceuticals USA, Inc.	DIAZEPAM	10 mg/1	500 TABLET in 1 BOTTLE (0172-3927-70)
0172-3927-80	0172-3927	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	19861210	N/A	ANDA	ANDA071322	Teva Pharmaceuticals USA, Inc.	DIAZEPAM	10 mg/1	1000 TABLET in 1 BOTTLE (0172-3927-80)
71335-0444-0	71335-0444	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20240403	N/A	ANDA	ANDA071322	Bryant Ranch Prepack	DIAZEPAM	10 mg/1	56 TABLET in 1 BOTTLE (71335-0444-0)
71335-0444-1	71335-0444	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20190726	N/A	ANDA	ANDA071322	Bryant Ranch Prepack	DIAZEPAM	10 mg/1	20 TABLET in 1 BOTTLE (71335-0444-1)
71335-0444-2	71335-0444	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20180214	N/A	ANDA	ANDA071322	Bryant Ranch Prepack	DIAZEPAM	10 mg/1	30 TABLET in 1 BOTTLE (71335-0444-2)
71335-0444-3	71335-0444	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20180227	N/A	ANDA	ANDA071322	Bryant Ranch Prepack	DIAZEPAM	10 mg/1	40 TABLET in 1 BOTTLE (71335-0444-3)
71335-0444-4	71335-0444	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20240403	N/A	ANDA	ANDA071322	Bryant Ranch Prepack	DIAZEPAM	10 mg/1	50 TABLET in 1 BOTTLE (71335-0444-4)
71335-0444-5	71335-0444	HUMAN PRESCRIPTION DRUG	Diazepam	Diazepam	TABLET	ORAL	20180219	N/A	ANDA	ANDA071322	Bryant Ranch Prepack	DIAZEPAM	10 mg/1	60 TABLET in 1 BOTTLE (71335-0444-5)